Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians (2008)
- Authors:
- Autor USP: ISAAC, LOURDES - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Investigative Ophthalmology and Visual Science
- Volume/Número/Paginação/Ano: v. 49, 2008
- Conference titles: Annual Meeting of the Association for Research in Vision and Ophthalmology - ARVO
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ABNT
TEIXEIRA, A. et al. Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians. Investigative Ophthalmology and Visual Science. St. Louis: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 11 jan. 2026. , 2008 -
APA
Teixeira, A., Silva, A. S., Lin, F. L. H., Isaac, L., & Belfort, R. (2008). Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians. Investigative Ophthalmology and Visual Science. St. Louis: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Teixeira A, Silva AS, Lin FLH, Isaac L, Belfort R. Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians. Investigative Ophthalmology and Visual Science. 2008 ; 49[citado 2026 jan. 11 ] -
Vancouver
Teixeira A, Silva AS, Lin FLH, Isaac L, Belfort R. Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians. Investigative Ophthalmology and Visual Science. 2008 ; 49[citado 2026 jan. 11 ] - Ligação de leptospira interrogans serovar pomona às diferentes variantes de fator H (TYR402 and HIS402)
- Intravitreal levels of human complement factor F (CFH) in patients with exudative age-related macular degeneration (AMD)
- Associação entre polimorfismo de fator H (Y402H) e degeneração da mácula relacionada à idade
- ARG 127 his substitution in SCR-2 of the regulatory complement protein factor H is found in a factor H deficient patient with concomitant lack of complement component C9
- Characterization and genetic analysis of human complement Factor I deficiency
- Immunological and genetic characterization of deficiency of the component C5 of the human complement system
- Human complement factor H (Y402H) polymorphism and age-related macular degeneration (AMD) in brazilian patients
- A missense mutation is associated with the regulatory complement protein factor H deficiency in a patient with concomitant lack of complement component C9
- Leptospira Immunoglobulin-like proteins bind human complement regulator Factor H
- The contribution of the component C5 in fatty liver disease: a murine model
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